Looking for Statistical Programmer jobs in Ahmedabad? Veeda CR is hiring experienced Statistical Programmers for its Clinical Data and Biostatistics team. This opportunity is ideal for professionals with 1–3 years of experience in Clinical SAS Programming, CDISC standards, SDTM, ADaM, Pinnacle 21, and Clinical Trials.

Candidates with a B.Pharm degree and hands-on experience in regulatory-compliant clinical programming will have an excellent opportunity to work on global clinical studies while preparing submission-ready datasets for regulatory authorities.

If you are searching for SAS Programmer jobs in India, Clinical SAS jobs, CDISC programming jobs, or Statistical Programmer vacancies in Ahmedabad, this opening is worth considering.

Job Overview

Key Responsibilities

The selected Statistical Programmer will be responsible for:

• Preparing Annotation CRFs using Adobe Acrobat Professional.
• Creating SDTM and ADaM mapping specification sheets.
• Developing and maintaining Clinical SAS programs.
• Preparing CDISC-compliant databases for regulatory submissions.
• Creating Define.xml using Pinnacle 21.
• Preparing SDTM aCRF documentation.
• Developing cSDRG and ADRG reports according to FDA guidelines.
• Using SAS Macros to automate repetitive programming tasks.
• Running Pinnacle 21 validation and resolving validation findings.
• Performing data validation checks.
• Collaborating with cross-functional stakeholders.
• Responding to QA observations within defined timelines.
• Completing internal SOP and Clinical Learning Program (CLP) training.

Required Qualifications

Applicants should have:

• Bachelor of Pharmacy (B.Pharm)
• 1–3 years of Statistical Programming experience
• Strong knowledge of:
  • Clinical SAS Programming
  • SAS Macros
  • CDISC Standards
  • SDTM
  • ADaM
  • Define.xml
  • Pinnacle 21
  • FDA submission standards
  • Clinical Trial Data Management

Preferred Skills

• SAS Programming
• Clinical SAS
• SDTM Programming
• ADaM Dataset Development
• CDISC Implementation
• Metadata Creation
• Define.xml Generation
• Pinnacle 21 Validation
• Clinical Trial Programming
• Regulatory Submission Support

Why Join Veeda CR?

Working at Veeda CR offers professionals the opportunity to:

• Work on global clinical research projects.
• Gain experience with FDA-compliant regulatory submissions.
• Enhance expertise in CDISC implementation.
• Build advanced SAS programming skills.
• Collaborate with experienced clinical research professionals.
• Grow within a leading Clinical Research Organization (CRO).

Salary

Based on experience and industry standards, the expected salary ranges between:

₹4,00,000 – ₹6,50,000 per annum (CTC)

Who Should Apply?

This opportunity is suitable for professionals with experience in:

• Clinical SAS Programming
• Statistical Programming
• CDISC Implementation
• SDTM Dataset Creation
• ADaM Programming
• Regulatory Submission Programming
• Clinical Data Standards
• Clinical Trial Programming

How to Apply

Application Link